HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874007Generated: October 30, 2026
Diisopropylethylamine → Tert-butyl 5-(methylcarbamoyl)thiazol-2-ylcarbamate
https://huagongshe.com/reaction/1874007
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 2-N-Boc-Amino-Thiazole-5-Carboxylic Acid | HCID 22271442 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Tert-butyl 5-(methylcarbamoyl)thiazol-2-ylcarbamate | HCID 86649520 | 73% |
Reaction Steps
To a heterogeneous mixture of 2-(tert-butoxycarbonylamino)thiazole-5-carboxylic acid (1.0 g, 4.1 mmol), 1-hydroxybenzotriazole hydrate (0.63 g, 4.1 mmol), N,N-diisopropylethylamine (4.3 mL, 24 mmol), methylamine hydrochloride (0.83 g, 12 mmol) in anhydrous acetonitrile (20 mL), was added WSCDI (2.4 g, 12 mmol) at room temperature under a nitrogen atmosphere and stirred at room temperature overnight. The reaction mixture was concentrated in vacuo. To the residue was added saturated aqueous sodium bicarbonate solution (20 mL), ethyl acetate (6 mL), and heptane (2 mL). The solid that separates out was filtered, washed with water (2×2 mL) and diethyl ether (2×4 mL), and dried to give tert-butyl 5-(methylcarbamoyl)thiazol-2-ylcarbamate (0.77 g, 73% yield) as a white solid. MS found: (M+H)+=258; 1H NMR (400 MHz, methanol-d4) δ ppm 7.83 (s, 1H), 2.87 (s, 3H), 1.55 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304539B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-4b75c05436cc4bc0a166d7589795cc22 |
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| Source note | uspto-grants-2012_11 |
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